Výsledky vyhledávání - "Louis C K Low"

Growth of children with β-thalassemia major

Autor: Louis C K Low

Publikováno v: The Indian Journal of Pediatrics. 72:159-164

Hypertransfusion and regular chelation therapy have allowed improved survival in patients with thalassemia major (TM). Despite medical advances, growth failure and hypogonadism remain significant clinical problems in these patients in adolescence. Di

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85fe7ba6bc172f9921c532a5b2ae9a71
https://doi.org/10.1007/bf02760702

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A Follow-Up Study of Adherence and Glycemic Control Among Hong Kong Youths With Diabetes

Autor: Carroll W. Hughes, Louis C K Low, Sunita M. Stewart, Peter W. H. Lee, Kwai Fun Huen, David A. Waller, Betsy D. Kennard, Anna Cheng

Publikováno v: Journal of Pediatric Psychology. 28:67-79

Objective To extend longitudinally an earlier study of the pathway from symptoms of emotional distress (ED) through self-efficacy (SE) and adherence to glycemic control (GC) in youths with diabetes, and to examine the contribution of different specif

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https://doi.org/10.1093/jpepsy/28.1.67

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Goitrogenesis during pregnancy and neonatal hypothyroxinaemia in a borderline iodine sufficient area

Autor: Louis C K Low, MT Chau, Sidney Tam, Awc Kung, T. T. Lao

Publikováno v: Clinical Endocrinology. 53:725-731

OBJECTIVE: Severe iodine deficiency disorders (IDDs) may have been eradicated in many parts of the world, but milder forms still exist and may escape detection. We evaluated the impact of pregnancy on the maternal and fetal thyroid axis in Hong Kong,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e00b54e9a24b1c609a372fdef0e8c9fb
https://doi.org/10.1046/j.1365-2265.2000.01156.x

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Serum growth hormone (GH) binding protein, IGF-I and IGFBP-3 in patients with β-thalassaemia major and the effect of GH treatment

Autor: Louis C K Low, M. C. Postel-Vinay, P. T. Cheung, E. Y. W. Kwan

Publikováno v: Clinical Endocrinology. 48:641-646

OBJECTIVE Levels of IGFI have been shown to be low in transfusion-dependent thalassaemia and there is preliminary evidence to suggest that this may be reversed by GH treatment. In this further study we have evaluated serum growth hormone (GH) binding

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8e346e580a4c3d0088062583c47d566c
https://doi.org/10.1046/j.1365-2265.1998.00470.x

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Iodine insufficiency and neonatal hyperthyrotropinaemia in Hong Kong

Autor: Annie W.C. Kung, R. W. C. Pang, J. D. Robinson, Louis C K Low, Terence T. Lao

Publikováno v: Clinical Endocrinology. 46:315-319

OBJECTIVES 23% of the neonatal hypothyroidism in Hong Kong is transient. The present study aims to evaluate iodine excretion in healthy pregnant women in Hong Kong and to determine whether iodine insufficiency may occur in the local population to acc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6f216a6dd302842068689b71eaaa792
https://doi.org/10.1046/j.1365-2265.1997.1310960.x

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An episode of syncope attacks in adolescent schoolgirls: Investigations, intervention and outcome

Autor: Wing Cheong Leung, Patrick W. L. Leung, Amy S. M. Fung, M. C. Tsang, Louis C K Low, Peter W. H. Lee

Publikováno v: British Journal of Medical Psychology. 69:247-257

An increasing number of students in a secondary convent girls school developed syncope attacks over a time course of about two months. Fourteen students who suffered from syncope and 12 other students from the same class with no symptoms were assesse

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https://doi.org/10.1111/j.2044-8341.1996.tb01867.x

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Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiency

Autor: Chun-Hung Ko, Ching-Wan Lam, Joannie Hui, Louis C K Low, K Y Chan, Chloe Miu Mak, Eric Kin-Cheong Yau, Cheuk-Wing Fung, Simon T.S. Siu, WL Yeung, Virginia Wong

Publikováno v: Journal of child neurology. 26(2)

This study included 12 Chinese patients with a wide spectrum of phenotypes of tyrosine hydroxylase deficiency. Seven females and 5 males, aged 2.2 to 41 years, had phenotypes ranging from severe type with onset at infancy to mild type with onset afte

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7750983b71fe29d630104a6efbe2ad5e
https://pubmed.ncbi.nlm.nih.gov/20823027

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Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese

Autor: Hon Cheung Lee, Chun-Hung Ko, Yan-Wo Chan, Chloe Miu Mak, Virginia Wong, Yuet-Ping Yuen, Sidney Tam, S.P. Chen, Sui-Fan Tong, WL Yeung, Cheuk-Wing Fung, Ching-Wan Lam, Tak-Shing Siu, B Chan, Joannie Hui, Louis C K Low, KY Chan, E. Yau, Wai-Kwan Siu

Publikováno v: Molecular genetics and metabolism. 99(4)

Tyrosine hydroxylase deficiency is a rare neurotransmitter disorder affecting the rate-limiting step in catecholamine biosynthesis. There are about 40 cases reported worldwide. Here, we report the biochemical and molecular findings of eight unrelated

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29deccfbfc85f8660ab1949b4cebd2a1
https://pubmed.ncbi.nlm.nih.gov/20056467

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